Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Di(succinimido) carbonate | HCID 676246 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86657248 | HCID 86657248 | 11.1% |
Reaction Steps
To methyl acetate (0.600 g, 8.1 mmol) and Ti(O-iPr)4 (0.15 g, 0.43 mmol) in ether (30 mL) was added dropwise EtMgBr (3.0M in ether, 6.0 mL, 18 mmol) over a hour period. After stirring for 20 minutes, the mixture was poured onto 10% H2SO4 (80 mL) and extracted with ether. The ether was dried over MgSO4 and concentrated in vacuo (0° C.) to one-quarter volume. The resulting solution was diluted with MeCN (20 mL) and treated with disuccinimidyl carbonate (4.15 g, 16.2 mmol). After stirring for an additional 20 minutes. Et3N (3.4 mL, 25 mmol) was added. After stilling for an additional 24 hours, the mixture was partitioned with EtOAc and saturated NaHCO3, dried over MgSO4, filtered and concentrated in vacuo to provide 1-methylcyclopropyl hydroxysuccinimidyl carbonate as a yellow solid (0.191 g, 0.90 mmol) which was combined with compound 77A (0.190 g, 0.45 mmol) and Et3N (0.25 mL, 1.8 mmol) in CH2Cl, (5 mL). After stirring for 1 h, the reaction was concentrated and purified using PLC to provide compound 311 as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907095B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-53e89dbe08734a81a65c6aadc57035cd |
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| Source note | uspto-grants-2014_12 |
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